The circadian oscillator of the cerebral cortex: molecular, biochemical and behavioral effects of deleting the Arntl clock gene in cortical neurons

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Standard

The circadian oscillator of the cerebral cortex: molecular, biochemical and behavioral effects of deleting the Arntl clock gene in cortical neurons. / Bering, Tenna; Carstensen, Mikkel Bloss ; Wörtwein, Gitta; Weikop, Pia; Rath, Martin Fredensborg.

I: Cerebral Cortex, Bind 28, Nr. 2, 02.2018, s. 644–657.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Bering, T, Carstensen, MB, Wörtwein, G, Weikop, P & Rath, MF 2018, 'The circadian oscillator of the cerebral cortex: molecular, biochemical and behavioral effects of deleting the Arntl clock gene in cortical neurons', Cerebral Cortex, bind 28, nr. 2, s. 644–657. https://doi.org/10.1093/cercor/bhw406

APA

Bering, T., Carstensen, M. B., Wörtwein, G., Weikop, P., & Rath, M. F. (2018). The circadian oscillator of the cerebral cortex: molecular, biochemical and behavioral effects of deleting the Arntl clock gene in cortical neurons. Cerebral Cortex, 28(2), 644–657. https://doi.org/10.1093/cercor/bhw406

Vancouver

Bering T, Carstensen MB, Wörtwein G, Weikop P, Rath MF. The circadian oscillator of the cerebral cortex: molecular, biochemical and behavioral effects of deleting the Arntl clock gene in cortical neurons. Cerebral Cortex. 2018 feb.;28(2):644–657. https://doi.org/10.1093/cercor/bhw406

Author

Bering, Tenna ; Carstensen, Mikkel Bloss ; Wörtwein, Gitta ; Weikop, Pia ; Rath, Martin Fredensborg. / The circadian oscillator of the cerebral cortex: molecular, biochemical and behavioral effects of deleting the Arntl clock gene in cortical neurons. I: Cerebral Cortex. 2018 ; Bind 28, Nr. 2. s. 644–657.

Bibtex

@article{0243f7a439be4c8c86d7ddf5bfe5981e,
title = "The circadian oscillator of the cerebral cortex: molecular, biochemical and behavioral effects of deleting the Arntl clock gene in cortical neurons",
abstract = "A molecular circadian oscillator resides in neurons of the cerebral cortex, but its role is unknown. Using the Cre-LoxP method, we have here abolished the core clock gene Arntl in those neurons. This mouse represents the first model carrying a deletion of a circadian clock component specifically in an extrahypothalamic cell type of the brain. Molecular analyses of clock gene expression in the cerebral cortex of the Arntl conditional knockout mouse revealed disrupted circadian expression profiles, whereas clock gene expression in the suprachiasmatic nucleus was still rhythmic, thus showing that Arntl is required for normal function of the cortical circadian oscillator. Daily rhythms in running activity and temperature were not influenced, whereas the resynchronization response to experimental jet-lag exhibited minor though significant differences between genotypes. The tail-suspension test revealed significantly prolonged immobility periods in the knockout mouse indicative of a depressive-like behavioral state. This phenotype was accompanied by reduced norepinephrine levels in the cerebral cortex. Our data show that Arntl is required for normal cortical clock function and further give reason to suspect that the circadian oscillator of the cerebral cortex is involved in regulating both circadian biology and mood-related behavior and biochemistry.",
author = "Tenna Bering and Carstensen, {Mikkel Bloss} and Gitta W{\"o}rtwein and Pia Weikop and Rath, {Martin Fredensborg}",
year = "2018",
month = feb,
doi = "10.1093/cercor/bhw406",
language = "English",
volume = "28",
pages = "644–657",
journal = "Cerebral Cortex",
issn = "1047-3211",
publisher = "Oxford University Press",
number = "2",

}

RIS

TY - JOUR

T1 - The circadian oscillator of the cerebral cortex: molecular, biochemical and behavioral effects of deleting the Arntl clock gene in cortical neurons

AU - Bering, Tenna

AU - Carstensen, Mikkel Bloss

AU - Wörtwein, Gitta

AU - Weikop, Pia

AU - Rath, Martin Fredensborg

PY - 2018/2

Y1 - 2018/2

N2 - A molecular circadian oscillator resides in neurons of the cerebral cortex, but its role is unknown. Using the Cre-LoxP method, we have here abolished the core clock gene Arntl in those neurons. This mouse represents the first model carrying a deletion of a circadian clock component specifically in an extrahypothalamic cell type of the brain. Molecular analyses of clock gene expression in the cerebral cortex of the Arntl conditional knockout mouse revealed disrupted circadian expression profiles, whereas clock gene expression in the suprachiasmatic nucleus was still rhythmic, thus showing that Arntl is required for normal function of the cortical circadian oscillator. Daily rhythms in running activity and temperature were not influenced, whereas the resynchronization response to experimental jet-lag exhibited minor though significant differences between genotypes. The tail-suspension test revealed significantly prolonged immobility periods in the knockout mouse indicative of a depressive-like behavioral state. This phenotype was accompanied by reduced norepinephrine levels in the cerebral cortex. Our data show that Arntl is required for normal cortical clock function and further give reason to suspect that the circadian oscillator of the cerebral cortex is involved in regulating both circadian biology and mood-related behavior and biochemistry.

AB - A molecular circadian oscillator resides in neurons of the cerebral cortex, but its role is unknown. Using the Cre-LoxP method, we have here abolished the core clock gene Arntl in those neurons. This mouse represents the first model carrying a deletion of a circadian clock component specifically in an extrahypothalamic cell type of the brain. Molecular analyses of clock gene expression in the cerebral cortex of the Arntl conditional knockout mouse revealed disrupted circadian expression profiles, whereas clock gene expression in the suprachiasmatic nucleus was still rhythmic, thus showing that Arntl is required for normal function of the cortical circadian oscillator. Daily rhythms in running activity and temperature were not influenced, whereas the resynchronization response to experimental jet-lag exhibited minor though significant differences between genotypes. The tail-suspension test revealed significantly prolonged immobility periods in the knockout mouse indicative of a depressive-like behavioral state. This phenotype was accompanied by reduced norepinephrine levels in the cerebral cortex. Our data show that Arntl is required for normal cortical clock function and further give reason to suspect that the circadian oscillator of the cerebral cortex is involved in regulating both circadian biology and mood-related behavior and biochemistry.

U2 - 10.1093/cercor/bhw406

DO - 10.1093/cercor/bhw406

M3 - Journal article

C2 - 28052921

VL - 28

SP - 644

EP - 657

JO - Cerebral Cortex

JF - Cerebral Cortex

SN - 1047-3211

IS - 2

ER -

ID: 170135557